All recall categories

Labeling and dosing error recalls

Nothing is contaminated in these recalls — the package says the wrong thing. That can mean a bottle holding a different strength than the label states, two products packed in the wrong carton, or missing directions. For medication these can matter as much as contamination, because the dose taken is the wrong one.

983 stored notices, reported between Jun 20, 2012 and Nov 11, 2026. Newest first.

Medical devices

Reported Mar 15, 2017

MicroAire K-Wires

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MicroAire Surgical Instruments, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

OP7543 Design Y Mandible Onlay - Medium - Left and OP7544 Design Y Mandible Onlay - Medium - Right

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Matrix Surgical Holdings, LLC

FDA (openFDA device enforcement)

Drugs

Reported Mar 1, 2017

Levothyroxine Sodium 135 mcg/Liothyronine 15 mcg SR capsules, 90 count bottles, Rx only, Moore's Pharmacy Compounding,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Moore's Compounding Pharmacy

FDA (openFDA drug enforcement)

Drugs

Reported Feb 15, 2017

Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9;…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Apotex Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 8, 2017

Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien LLC

FDA (openFDA device enforcement)

Drugs

Reported Feb 8, 2017

Endure 400 Scrub-Stat (chlorhexidine gluconate) Foam Forming Solution, 4%, packaged in plastic (HDPE) bottles,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Ecolab, Inc.

FDA (openFDA drug enforcement)

Food

Reported Feb 8, 2017

Whole Foods Markets Lobster Bisque Distributed by: Whole Foods Market, Englewood Cliffs, NJ 07652 UPC: 8-80632-00100

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Whole Foods Market Northeast Regional Office

FDA (openFDA food enforcement)

Medical devices

Reported Feb 8, 2017

Orthopedic Salvage System (OSS) 9cm prosthesis, knee, femorotibial, constrained, cemented, metal/polymer Knee System…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Jan 31, 2017

Teufelberger Recalls Rescue Ropes and Throwlines Due to Fall and Injury Hazards

High riskUsing this product could cause serious injury, illness or death — stop using it now.

TEUFELBERGER Fiber Rope Corp.

CPSC

Drugs

Reported Jan 25, 2017

Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets),…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Novum Pharma, LLC

FDA (openFDA drug enforcement)

Drugs

Reported Jan 25, 2017

Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Sandoz Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Jan 25, 2017

HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding &…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Town and Country Compounding and Consultation Services, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 18, 2017

i.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Health Robotics S.r.l.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2017

Oxford Fixed Lateral Bearing Size F Right, Part Number 154375 Lot 744260, Sterile, The product is placed into an…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 4, 2017

INOVA (benzoyl peroxide) 4%, Easy Pad (tocopherol) 5%, For topical use only, packaged in a box containing: 30 pads of…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Cipher Pharmaceuticals US LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 28, 2016

Zeus-P Lumbar Interbody Device

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amendia, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Dec 28, 2016

Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Virtus Pharmaceuticals Opco Ii L

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 21, 2016

ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable, Contents: Five (5) Disposable Bipolar Cables,STERILE The Minor…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ellman International, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 21, 2016

Clear plastic cup labeled as: The Farmers Market Buffalo Hot Peanuts; Net Wt. 5 oz.; UPC 3003499846; Best By 10/25/2016

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Giant Eagle, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2016

Empowr Knee System Product Usage: Non-porous proximal tibial baseplate implants, utilized in either posterior cruciate…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2016

UltraSeal XT Plus Clear Refill. The package contains 4x 1.2 ml UltraSeal XT Plus. Product Usage: The UltraSeal XT Plus…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 14, 2016

SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION, 62.5mg elemental iron/5mL, 10 (5mL vials) per shelf pack, Rx…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

West-Ward Pharmaceuticals Corp.

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 7, 2016

ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System, Sterile Catalog Number: TCR-111-1111. Intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ConforMIS, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Nov 30, 2016

LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pfizer Inc.

FDA (openFDA drug enforcement)

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Related categories

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.